Patients with early onset of type 1 diabetes have significantly higher GG genotype at position 49 of the CTLA4 gene

Type 1 diabetes (T1D) is a complex autoimmune disease. Several genetic loci have been implicated in the susceptibility to this illness. Evaluated was the role of the CTLA4 exon 1 A49G polymorphism and its role as a risk factor for T1D in our population. DNA from 190 patients with T1D and their famil...

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Veröffentlicht in:Human immunology 2004-07, Vol.65 (7), p.719-724
Hauptverfasser: Zalloua, Pierre A., Abchee, Antoine, Shbaklo, Hadia, Zreik, Tony G., Terwedow, Henry, Halaby, Georges, Azar, Sami T.
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Sprache:eng
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Zusammenfassung:Type 1 diabetes (T1D) is a complex autoimmune disease. Several genetic loci have been implicated in the susceptibility to this illness. Evaluated was the role of the CTLA4 exon 1 A49G polymorphism and its role as a risk factor for T1D in our population. DNA from 190 patients with T1D and their families and 96 control individuals were genotyped for CTLA4 exon 1 polymorphism and human leukocyte antigen (HLA)–DQB1*0201 and *0302 haplotypes by polymerase chain reaction (PCR) amplification–restriction enzyme analysis and PCR amplification that used sequence-specific primers, respectively. Patients were nonobese and
ISSN:0198-8859
1879-1166
DOI:10.1016/j.humimm.2004.04.007